A characteristic feature of the menopause is a marked attenuation in the production and release of ovarian steroids, such as estradiol and progesterone. However, the impact of these changes on human physiology, especially within the central nervous system (CNS), is far from being clear. We have already shown that female rhesus macaques, like women, undergo menopause, and that a change in plasma FSH and inhibin B levels represents the first endocrine manifestation of this event. We have also shown that plasma levels of the adrenal steroid, dehydroepiandrosterone (DHEA), fall markedly around this time. DHEA is one of the most abundant steroids in the circulation;it is released into the circulation in a circadian manner and is readily converted to estradiol in many tissues. The overall aim of this proposal is to examine the interacting impact of adrenal and ovarian aging on the CNS of primates. Using the female rhesus macaque as a pragmatic animal model, we propose to test the hypothesis that the aging-related attenuation of DHEA release exacerbates the perimenopausal decline in estradiol, and thereby negatively impacts central physiological processes such as cognition, learning, and attention, and leads to perturbation of the circadian sleep-wake cycle.
Specific Aim 1 will use a battery of behavioral tests to assess differences between young adults, old regularly-cycling and irregularly-cycling adults, and old ovariectomized adults;the old animals will be tested both as untreated controls and also after extended treatment with """"""""young"""""""" physiological levels of DHEA. Cognitive and behavioral assessments will include: 1) delayed response test of spatial working memory, which is particularly sensitive to aging and prefrontal cortex dysfunction;2) delayed non- matching-to-sample, a task probing primarily hippocampus-based memory;3) a visuospatial cueing test of visual attention that is estrogen-sensitive;and 4) a test of behavioral reactivity sensitive to amygdala damage. In addition, sleep-wake cycles will be continuously monitored using Actiwatch recorders, and MRI will be performed before and after DHEA replacement to monitor morphological and biochemical changes in the key brain regions.
Specific Aim 2 will use a series of biochemical and histochemical methodologies to elucidate the plasticity that occurs within the CNS during adrenal-ovarian aging. Gene microarrays and RT-PCR will be used to identify genes that are differentially expressed in the CNS between young and old animals, regular and irregular old cyclers, and DHEA-treated and untreated old animals. The focus will be on genes encoding enzymes involved in the conversion of DHEA to estradiol, steroid receptors, and genes associated with key neurotransmitters systems and circadian clocks. Immunohistochemistry, in situ hybridization histochemistry, RIA and biochemical enzymology will be used to corroborate the results. By elucidating the interacting impact of declining ovarian and adrenal steroids on CNS function, we expect to lay a foundation for the development of therapies for many aging-associated disorders in women.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Project (R01)
Project #
5R01AG029612-04
Application #
7917302
Study Section
Special Emphasis Panel (ZRG1-EMNR-E (02))
Program Officer
Mackiewicz, Miroslaw
Project Start
2007-09-01
Project End
2012-08-31
Budget Start
2010-09-01
Budget End
2011-08-31
Support Year
4
Fiscal Year
2010
Total Cost
$378,373
Indirect Cost
Name
Oregon Health and Science University
Department
Other Basic Sciences
Type
Schools of Medicine
DUNS #
096997515
City
Portland
State
OR
Country
United States
Zip Code
97239
Eghlidi, Dominique H; Luna, Selva L; Brown, Donald I et al. (2018) Gene expression profiling of the SCN in young and old rhesus macaques. J Mol Endocrinol 61:57-67
Sorwell, K G; Renner, L; Weiss, A R et al. (2017) Cognition in aged rhesus monkeys: effect of DHEA and correlation with steroidogenic gene expression. Genes Brain Behav 16:361-368
Aghazadeh-Sanai, Nona; Downs, Jodi L; Mattison, Julie A et al. (2017) Effect of caloric restriction on plasma melatonin levels in aged rhesus macaques. Neurobiol Aging 55:213-216
Urbanski, Henryk F; Sorwell, Krystina G; Prokai, Laszlo et al. (2017) Effect of short-term DHEA supplementation on serum and hippocampal estrogen concentrations in perimenopausal female rhesus macaques. Neurobiol Aging 55:172-174
Luna, Selva L; Brown, Donald I; Eghlidi, Dominique H et al. (2017) Locomotor activity and the expression of orexin A and orexin B in aged female rhesus macaques. Neurobiol Aging 50:1-4
Eghlidi, Dominique H; Garyfallou, Vasilios T; Kohama, Steven G et al. (2017) Age-associated gene expression changes in the arcuate nucleus of male rhesus macaques. J Mol Endocrinol 59:141-149
Urbanski, Henryk F; Mueller, Kevin; Bethea, Cynthia L (2017) Effect of an obesogenic diet on circadian activity and serum hormones in old monkeys. Endocr Connect 6:380-383
Bethea, Cynthia L; Kohama, Steven G; Reddy, Arubala P et al. (2016) Ovarian steroids regulate gene expression in the dorsal raphe of old female macaques. Neurobiol Aging 37:179-191
Burton, Katherine J; Li, Xiaohan; Li, Baoan et al. (2016) Expression of prokineticin 2 and its receptor in the macaque monkey brain. Chronobiol Int 33:191-9
Eghlidi, Dominique H; Urbanski, Henryk F (2015) Effects of Age and Estradiol on Gene Expression in the Rhesus Macaque Hypothalamus. Neuroendocrinology 101:236-45

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